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By J. E. Murphy

Neodymium was electrowon into a Mg-Cd molten cathode at 650 °C from NdC1,-KC1 electrolyte. With the chloride system, neodymium was deposited into the molten alloy cathode until the neodymium concentration reached 20 wt pct. The alloy was then vacuum melted to remove the Mg and Cd. The current efficiency exceeded 80 pct under optimum conditions and the purity of the metal was 99.9 pct after vacuum melting. As an alternative approach, neodymium was electrowon at 1,030 °C from Nd,O, dissolved in a molten fluoride eleotrolyte. With the oxide-fluoride electrolyte, the metal was electrowon in a molten state with current efficiencies up to 60 pct. The purity of the metal was 99.8 pct with oxygen and carbon as major impurities. A number of problems were encountered including anode effect, low oxide solubility in the electrolyte, high neodymium metal solubility in the electrolyte, and reactivity of the metal with the cell materials. Approaches to improved cell, operation and prospects for commercial adoption of the electrolytic production of neodymium metal are discussed.

Jan 1, 1995

By Sergei A. Degterov

A thermodynamic database for the slag, matte and liquid copper phases in the Cu-Ca-Fe-Pb-Zn-Si-O-S system has been developed for the ranges of compositions of importance to the production of copper. When used with the Gibbs energy minimization software and other databases of the F*A*C*T thermodynamic computing system, this database will permit the calculation of matte-slag-copper-gas phase equilibria that take place during copper smelting and converting. The calculations reproduce within experimental error limits all available experimental data on phase diagrams, activities of components, enthalpies of mixing, matte - alloy miscibility gap and tie-lines. The calculated solubilities of Cu in both S-free slag and slag equilibrated with matte are also in good agreement with experiment under all studied conditions, such as at SiO2 saturation, in equilibrium with Fe, Cu or Cu-Au alloys, at fixed oxygen or SO2 partial pressures and at different contents of Pb, Zn and CaO in the slag. Sulfide contents (sulfide capacities) of the slags are predicted within experimental error limits. The distribution of Pb and Zn among matte, slag, copper and gas has been calculated. The calculations are in good agreement with experimental data and predict the distributions under conditions which are difficult to study experimentally, such as at magnetite saturation or under various oxygen partial pressures and iron to silica ratios in the slag.

Jan 1, 1999

By Manolete Mena

WC-Co nanocomposite powder is among the first group of materials with a promising potential for nanocrystalline-materials application. A chemical vapor synthesis (CVS) process that has previously been used for preparing the aluminides of titanium and nickel, and other metallic and intermetallic powders has been applied to the preparation of WC-Co nanocomposite powder. This CVS system was designed so that a tungsten precursor (WCl6 powder) and a cobalt precursor (CoCl2 powder) were separately fed into each evaporator in a reactor by means of specially designed powder feeders. The reduction and carburization of the vaporized chlorides by methane-hydrogen mixtures produced nanosized WC and Co composite powder. The product is a very uniform mixture of the constituent powders, which is important to ensure a high quality of the bulk cemented tungsten carbide product after consolidation. In the present work, the effects of reaction temperature, CH4 to WCl6 ratio, CH4 to H2 ratio, residence time, and Co content on the powder composition and particle size were determined. The products were characterized using XRD, carbon analyzer, and TEM.

Jan 1, 2006

By P. Chris Pistorius

Calcium treatment of alumina inclusions, to convert the alumina to molten or partially molten calcium aluminates, is a well-established treatment for steel, to improve the castability of aluminium-killed steel. However, the role of magnesium in calcium-treated steel is not fully clear, nor is the origin of the several percent of magnesium oxide that is often present in calcium-treated inclusions. To study this, steel was sampled after calcium treatment at an industrial steel plant, and the inclusions identified by energy-dispersive X-ray microanalysis (EDX) on polished sections of the samples (analysing the samples in a scanning electron microscope). The predicted fraction liquid in the inclusion was estimated from the ternary alumina-magnesia-lime phase diagram. Inclusions with higher CaO contents generally had lower MgO contents, indicating that the calcium wire is not the origin of the magnesium in the inclusions; this was also confirmed by wet chemical analysis of the calcium wire. Instead, it appears that magnesium-alumina spinel inclusions form during extended ladle contact after aluminium killing and before calcium treatment. While such spinels have been stated to cause poor castability (clogging the submerged-entry nozzle), it is clear that calcium treatment successfully modifies the spinel inclusions to mixed alumina-lime-magnesia inclusions, where the magnesia content contributes substantially to liquefaction of the inclusions: for typical MgO contents of around 10%, the range of Ca:O ratios which yield liquid (or partially liquid) inclusions is extended substantially to lower Ca:O ratios.

Jan 1, 2006

By Dinabandhu Ghosh

The stability diagram of the ternary system Ti-C-O is drawn in the present work for four temperatures, 1473 K, 1573 K, 1673 K and 1873 K, showing the stability fields of TiC, Ti, TiO, Ti2O3 and TiO2. An analysis of the system reveals that it is not possible to produce Ti in a carbon-saturated system; instead, the stable product is TiC. However, Ti can be an equilibrium product in a carbon-unsaturated system at prohibitively low values of pCO and pCO2; for example, at 1873 K, these limiting values are: pCO = 10-6.76 atm and pCO2 = 10-13.36 atm, which, when exceeded, produce TiC and TiO respectively. The magnesiothermic reduction is examined through the stability diagram (log pO2 vs. 1/T) of the system Ti-Mg-O, drawn for a number of pMg values, presenting the pairwise stability fields such as Mg(l) + Ti(s), Mg(v) + Ti(s), MgO(s) + Ti(s), etc. The diagram shows that magnesium reduction of TiO to Ti is possible only at T < 1641 K with pMg = 1 atm and only at T < 1569 K with pMg = 0.5 atm. An experimental scheme for Mg vapor reduction of TiO2 is proposed in which an argon stream is passed over a Mg(liquid) evaporator at temperature T1 (say, 1234 K); the resulting Ar-Mg mixture at 1 atm is subsequently flown over a bed of TiO2 at temperature T2. A thermodynamic analysis establishes that complete reduction to Ti is possible and that the best results are obtained when T1 = T2.

Jan 1, 2006

By Tiruttani Munikamal, Suresh Sundarraj

"A numerical model of the induction hardening process of steel cranks has been developed and the predicted results of temperature and phase distribution during this solid state phase transformation process are verified with experimental data from the literature. This heat treatment process involves heating the crank to the austenitic temperature range followed by rapid quenching in water to harden the surface of the crank. The model has been developed using ABAQUS, commercial FEA software. The formation of martensite, pearlite, and retained austenite phases are modeled and implemented through a user defined function in ABAQUS. A sensitivity study on the various process parameters affecting the amount of phase distribution has been carried out.IntroductionThe type of surface and sub-surface microstructure as well as the residual stresses that are present in a component after manufacturing, significantly affects it fatigue performance. The wear resistance of the automotive components such as crankshaft, gears, camshaft and bearings depends on the surface hardness. In order to achieve the surface hardness, these steel components are subjected to a type of quench hardening heat treatment process. There are several heat treatment processes available for the industrial application to improve the mechanical properties of the final part. Case hardening using induction heating is one of the widely used industrial techniques for improving the surface microstructure of a steel component. It consists of two stages i.e. induction heating cycle, followed by quenching in a fluid medium (usually water or oil)"

Jan 1, 2012

By Ricardo Ponce

In recent years, ENAMI implemented modernisation plans at its two smelters in order to meet the government&apos;s environmental regulations introduced in the early 1990s. The modernisation plans defined the new SO2 and particulates emission targets, deadlines for compliance, and the revised treatment capacities of the smelters. At Las Ventanas smelter, the principal process change consisted of eliminating the reverberatory furnace. All the smelter feed is currently processed in a 4m diameter, 14m long Teniente Converter, using up to 34% oxygen enriched air. Dry concentrate is injected into the bath through tuyeres. A fuel oil burner compensates for any process heat deficiency. The Teniente Converter high copper content slag is cleaned in an electric furnace. This furnace is also used to melt internal reverts. This paper will discuss the successful operation of the slag cleaning electric furnace.

Jan 1, 1999

By C. M. Acuña

At the Chuquicamata Division of Codelco-Chile high arsenic concentrates are produced, which at the smelter are processed via the Outokumpu Flash Furnace and Teniente Converters to obtain copper mattes. In the case of the Teniente Converters the production of matte grade near white metal composition is a common practice since the eighties and provided in the pyrometallurgical route no appropiate measures are taken, penalties have to be paid because of arsenic content in the anodes. During smelting huge volume of slag is produced and elimination of arsenic by slagging at this step is not economically attractive. Although during fire refining is possible to eliminate arsenic by use of mixtures of calcium and sodium carbonates this alternative is expensive, takes long process time and decreases the lifetime of the refractory lining. In spite of these facts a reasonably way to control arsenic in metal, and therefore in the anode, is taking, action in the converting step. The effects of oxygen and arsenic content in metal, arsenic in white metal and basicity index of the slag upon the distribution coefficient of arsenic between metal and slag were investigated at pilot and industrial levels. The best results are obtained for metals around 7,000 ppm oxygen and 0.3 basicity index slag, which results in a 5.7 distribution coefficient for a 5,800 - 7,100 ppm arsenic content in white metal, 18%-24% CaO slag at 1473 - 1523K. Furthermore, no significant/visible refractory wear has been realized.

Jan 1, 1999

By Alex Moyano

At present, the Codelco Norte smelter processes in the Teniente Converter and the Flash smelting Furnace 1,420,000 t/y of its Chuquicamata concentrate with an arsenic content of up to 1.5%. In a near future Codelco-Chile is considering different processing options for a new projected concentrates from the Alejandro Hales mine (former Mansa Mina mine with an arsenic content of up to 6%). The main option is the possibility to process 3,000 t/d of mixing concentrates from the Alejandro Hales and the Chuquicamata mines, in the Teniente Converter. The main feature of this smelting unit will be high volatilization of arsenic when processing high arsenic-bearing concentrates. The CN smelter staff carried out a technical feasibility study to evaluate the processing of high arsenic-bearing concentrates directly in the Teniente Converter, thus the low arsenic-bearing concentrates can be processed in the FSF. Accordingly, laboratory scale tests were carried out at the Tohoku University facilities. The lab-scale results allowed an industrial scale test at the Codelco Norte smelter to smelt 2,300 tpd of high arsenic-bearing concentrates in the TC and evaluate the metallurgical impact in the smelting, converting and refining areas of the smelter. The main industrial-scale result confirmed the stabilization of the arsenic content at 0.5% in the 70% Cu produced white metal at the test condition.

Jan 1, 2006

By Lanre Oshinowo

The trend in process engineering is to design compact, more efficient processes, there is the paramount requirement to get the job done right the first time going from the drawing board to full-scale commercial operation. To accomplish this goal, there is also the need for tools beyond the traditional engineering toolkit to evaluate designs through virtual prototyping, thereby reducing the risks associated with making design decisions. One of the most important tools that has recently come to the forefront of process design and development is Computational Fluid Dynamics (CFD). CFD has been used at HATCH to address the key process parameters that drive the design of hydrometallurgical unit operations. This paper will detail the role of CFD at HATCH in achieving a superior level of confidence in the process design of autoclave circuits. Specifically, the optimum application of multiphase modeling including hydrodynamic, heat and mass transfer to hydrometallurgy operations, the impact of non-Newtonian slurry rheology on autoclave performance, and the challenges of optimizing the mixing of key reactants into slurries in autoclave reactors, is discussed.

Jan 1, 2003

By Heinz Boeni, Daniel Ott, Uca Silva

"Latin America is facing a rapid increase in internet use. Penetration with electronic equipment is in some countries approaching the level of industrialized countries. There is an evident need to resolve the management of “end-of-life” computers and other electronic equipment. Several studies in Latin America assessed the increasing e-waste quantities and confirmed the importance of a sustainable e-waste management. This paper gives an overview on the status on e-waste management in Latin America, explains the challenges for establishing an e-waste management system in a developing country setting and highlights the social and economic potential and the possibilities of a regional approach.IntroductionGlobal ICT-Trade and generation of e-waste from ICTThe global production of electronic devices and particularly of Information and Communication Technologies (ICT) faces the biggest industrial expansion of the history: OECD figures show that global trade of ICT technologies has reached 7.7% of the gross world product by 2004, the major proportion accruing from China [1]. In 2006 an estimated 230 million computers and 1 billion cell phones have been sold worldwide which corresponds to a volume of 5’848’000 t [2]. As a consequence, Waste from Electrical and Electronic Equipment (WEEE), or e-waste, is by far the fastest growing waste component. It reaches more than 5% referred to Municipal Solid Waste and e-waste generation in developing countries according to UNEP is expected to triple by 2010 [2].According to the OECD e-waste is “any appliance using an electric power supply that has reached its end-of-life” [3]. The European WEEE directive [4] distinguishes 10 categories of ewaste: Big household appliances, Small Household Appliances, IT and Telecommunications Equipment, Consumer Equipment, Lighting Equipment, Electrical and Electronic Tools, Toys, Leisure and Sports Equipment, Medical devices, Monitoring and Control Instruments, and Automatic dispensers. In this paper e-waste and WEEE are used as synonyms. Focus will be laid on e-waste from IT equipment (IT-waste), corresponding to category 3 of the European WEEEDirective."

Jan 1, 2008

At the present time, cyanide is the most widely used reagent to extract gold from its ores and concentrates. However, its use in mining has become the focus of intense attack by various groups throughout the world; as a consequence, a renewed effort has been launched to find suitable alternative lixiviants to recover gold. Chlorination was the most popular process to extract gold, before it was rendered obsolete with the advent of the cyanidation process at the turn of the last century, not least because it required the use of potentially hazardous and costly chlorine to oxidize/complex the gold. The PLASTOL® process, originally designed to recover the platinum group metals (PGM?s) from their ores and concentrates, provides an alternative to cyanide for gold ores. The process generates oxidizing conditions in the autoclave capable of forming the AuIII ion, and gold chloro-complexes result from the addition of small quantities (~5-10 g/L) of sodium chloride to the autoclave. The principles of the PLASTOL® process are briefly described, and several applications of the process to gold concentrates are presented. Various options available to recover gold from PLASTOL® leach solutions are also discussed.

Jan 1, 2003

By J. P. Ibáñez

The uptake of copper from extremely dilute aqueous solutions by alginate in the form of protonated dry alginate beads was investigated. Barium was used to cross link the alginate forming the beads. The effect of various experimental parameters such as pH and metal ions concentration on the uptake of copper were studied. The uptake was strongly dependent on the Cu-bearing solution pH up to a value of 4.5. A removal of 100% o was achieved when the initial concentration of copper was as low as 8.0 mg/L. The maximum uptake, i, e., the loading capacity, was found to be 167 mg of copper per g of beads. The mechanism governing the removal of copper was found to be ion exchange between protons of the alginate beads and cupric ions of the solution. For this ion exchange process a molar ratio, d[H+]/d[Cu2+], of 2.0 was determined. EPMA-EDX analysis of the Cu-loaded beads showed a uniform distribution of the ions throughout the structure of the alginate, regardless the solution pH. This may suggest that this sorbent material is a porous ion exchanger having high permeability and capacity. The uptake of copper and of the heavy metals cadmium and zinc by this sorbent is compared.

Jan 1, 1999

By Tracy Morris, Weldon Read, Luis Navarro

"During the leaching of anodic slimes, tellurium dissolves into the leach liquor together with copper and must be removed before the solution is sent to liberator cells for copper recovery. Prior to the installation of autoclaves, tellurium was precipitated using raw slimes that caused a recirculation of tellurium in the leaching circuit. After autoclaves were installed the old leach tanks were converted into tellurium reactors utilizing copper chips, steam and agitation to form a copper telluride precipitate. Tellurium levels of less than 10 rng/L are achieved in a timely manner.IntroductionThe electrolytic refining of copper consists of an electrolytic cell provided with an anode of impure copper, a cathode of substantially pure copper (starter sheet) and an electrolyte made of copper sulfate and sulfuric acid [1]. When a direct electrical current is passed between the anode and cathode inside the cell, the impure copper anode dissolves in the electrolyte and pure copper is plated onto the cathode. During this operation, many of the impurities are deposited on the bottom of the cell as an anodic slime residue composed of insoluble chemical compounds. Slimes are a major source of rare and precious metals in the copper industry [2-5],In the Amarillo Copper Refinery (ACR), the anodic copper slimes are sent to the Precious Metals department in order to extract and then refine the gold, silver, platinum and palladium from them. The remaining impurities, in the form of a soda slag or copper slag are sent to the Hayden smelter for further processing. Copper telluride is sent to the Selenium/Tellurium department inside the plant for selenium and tellurium recovery. During the leaching process of the anodic slimes, copper, tellurium, and other metal species in the slimes are dissolved into leach liquor that cannot be returned to the tankhouse unless the tellurium concentration is below 10 mg/L."

Jan 1, 2012

By T. Takasu

Overall productivity in copper refining is currently determined by the electrorefining process. Previous research showed that forced convection of the electrolyte improves the morphology of the copper deposit on the cathode and suppresses passivation of the anode. In this paper, electrorefining experiments under forced convection were carried out in the presence of As, Sb and Bi impurities, both in electrolyte and in the anode, to determine the effect of the impurities on the electrorefining process. The concentrations of the impurities in the deposit increased with increasing current density without forced convection. An increase in the fluid velocity suppressed the increase in impurity concentration. These concentrations were high, especially in the initial stage of deposition without forced convection, corresponding to a decrease in the cathode potential measured during that period. This indicates that the enrichment of impurities was induced electrochemically. The reason for the decrease in cathode potential was the low concentration of copper ions on the electrode surface because of ion consumption by the electrolysis. The forced convection of the electrolyte enhanced the ionic mass transfer and thus suppressed the polarization and deposition of the impurities. The fluid motion was shown to be effective in achieving electrolysis under high current density conditions.

Jan 1, 1999

By Kevin L. Purdy

The Process Technology Center of Phelps Dodge Mining Company (PDMC) .operates several test facilities in support of PDMC&apos;s hydrometallurgical operations. Installations for small leach columns, 15 cm. to 60 cm. (6 in. to 24 in.) in diameter, and large leach columns, 1.8 m. (6 ft.) in diameter, are complemented by a test facility for SX/EW operations. The history of and reasons for the development of these facilities: are described and original standard equipment is discussed. A primary goal in constructing these facilities was achieving a high degree of flexibility to allow for testing of new equipment and new leaching and SX/EW technologies as they are developed. Along with this challenge, construction of a filly integrated SX/EW test facility on a small scale brought its own set of challenges.

Jan 1, 1999

By Florian Kongoli

While calcium ferrite slags have been successfully used in continuous copper converting for the last 30 years, ferrous calcium silicate slag was proposed about 8 years ago as an additional alternative for copper smelting. Although both slags are normal extensions of each other their phase relations have not been completely clarified. In this paper the liquidus relations of both slags have been quantified at various areas that cover both of them. The existing experimental data have been first reviewed and discussed in relation to the solidification procedure. An original physical model is then used to predict various diagrams of the liquidus surface of both slags. It is shown that the ternary liquidus diagrams normally used for FeOx-SiO2-CaO system are not suitable for industrial slags. The new model diagrams of Fe/CaO versus SiO2 and Fe/SiO2 versus CaO as well as Fe/CaO versus Temperature and Fe/SiO2 versus temperature are proven to be much more convenient for ferrite and ferrous calcium silicate slags. Based on these diagrams the effect of SiO2 and CaO on the melting temperature is quantified. The effect of Cu2O is also quantified through the model. Some Fe/CaO versus Cu2O and Fe/SiO2versus CaO at various copper contents are predicted and the results show good agreement with the experimental data. It is also shown that in the presence of liquid copper, Cu2O is dissolved in the slag depending on the oxidation degree of the system and might lower the liquidus temperature. Some discussions are also presented taking into account plant observations and important conclusions are drawn for copper smelting and converting

Jan 1, 2006

By Christian Ludwig, Virginie Silberstein, Rizlan Bernier-Latmani, Simona Regenspurg

"Residues from waste incineration (bottom ashes) form large amounts of heavy metal-rich waste. Theoretically, heating and the addition of chloride to the ashes could remove these metals by formation of volatile metal chlorides. The remaining heavy metal-poor ashes could be used, for example, as cement additives. In the proposed process of our study we used bypass dust from the cement industry as chloride additives to the bottom ashes. We aim to determine experimentally the optimal conditions to remove heavy metals from ashes and to simulate this process by thermo- chemical modeling. In our experiment we investigate heavy metal flows by heating of differently composed mixtures of bottoms ash and bypass dust in dependence of different furnace temperatures (500-1200 °C). Furthermore, we investigate the reactivity (leaching characteristic) of the resulting product in order to predict if secondary residues can be landfilled in agreement to Swiss regulations for inert materials.IntroductionThe incineration of garbage is generally considered as the most environmentally friendly method for the reduction of municipal solid waste. This is because, compared to traditional storage of waste on landfills, incineration produces less greenhouse gases and destroys toxic organic compounds. The released exothermic energy can be recuperated and the residues from the combustion chamber (bottom ash) are strongly reduced in volume. However, they still form about 600 kt of waste per year in Switzerland, which needs to be landfilled. However, these residues could be potentially used as construction materials after mechanically recovering ferrous and non-ferrous metals. However, the resulting ashes (discharged dry or wet) still contain increased amount of heavy metals (exceeding state regulation) requiring them to be finally deposed on a hazardous waste site. A thermal treatment of these ashes could enable both, to separate and recuperate the remaining heavy metals and an inorganic heavy-metal poor material. The evaporation of metals depends on temperature and can be lowered by addition of chlorides, which would lower the boiling point of most metals by formation of metal chlorides (table 1). 745"

Jan 1, 2008

By Kaixi Jiang, Bangsheng Zhang, Lei Zhang, Haibei Wang, Xiaoping Zou

"China plays an important role in the global molybdenum industry; in fact, both China's molybdenum mine and smelter production ranked first in the world. The characteristics of China's molybdenum resources are quite complex, and moly-nickel ores with carbon, coppermoly ores and wulfenite can be only found in China. This paper firstly introduces China's molybdenum resource/ reserve situation. Secondly, the status of molybdenum smelting technologies, especially roasting by rotary kilns and multiple-hearth furnaces, are discussed. The practices and the development of some new technologies, such as pressure leaching, solvent extraction, ion exchange, carbon adsorption for moly-nickel ores and low grade molybdenite concentrates, are also introduced.IntroductionMolybdenum is widely used in special steels, aviation, alloys, chemistry, electronic and medical industries because of its excellent physical and chemical characters [1,2].In nature, molybdenum exists mainly as molybdenite associated with copper ore which are the main material for smelting. About 99% of molybdenum is produced from molybdenite. In addition, wulfenite, molybdenum oxide ore and graphite shale containing Mo-Ni have also industrial value to extract molybdenum and other metals such as Ni, Re, Pb and Zn. The reserves of molybdenum in China are about 8.4 million tons metal; China is ranked as the second largest source in the world. The output in China is more than 40 kt in 2010. Ferromolybdenum is the main product and then ammonium molybdate. The consumption in China is about 20 kt and the rest is exported to overseas.The first molybdenum smelter in China was built in 1963. Today the main producers include Jinduicheng Moly Company, Luanchuan Moly Company and Jiangxi Copper Group Company. Technologies and equipment have changed greatly. Roasting and multi-hearth furnaces are widely used. Several new processes were developed such as pressure leaching, solvent extraction, ion exchange and carbon absorption [3-8]."

Jan 1, 2012

By M. E. Reed

Clyde Materials Handling (CMH) and WorleyParsons have developed a concept for a flash furnace feed system using the specialist pneumatic conveying equipment expertise of CMH and the flash furnace process experience of WorleyParsons. CMH has developed a proprietary volumetric feeder (called a Rotofeed) which is extremely accurate and overcomes many of the problems inherent with loss-in-weight screw feeders and drag chain conveyors, previously regarded as state-of-the-art. Initial indications are that the Clyde-WorleyParsons Feed System could deliver the following benefits to Flash Furnace operation: ? Accurate pulse-less delivery of feed material to the head of the burner leading to improved combustion performance and process stability; ? Highly accurate split to the individual quadrants of a conventional burner tube, or provision of a smooth hollow curtain to a burner without guide vanes; ? Decreased pressure pulsation in the furnace due to improved combustion control and performance; ? Decreased temperature fluctuations in the furnace due to improved combustion characteristics and hence reductions in refractory thermal stress and wear; Plant measurements have indicated a correlation between the discharge of concentrate from the drag chain conveyor and high speed pressure fluctuations in the flash furnace settler. Pilot scale test have been conducted to illustrate that the system delivers pulse-less feed to the burner with even feed distribution axially.

Jan 1, 2006